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This role involves local scientific literature monitoring for adverse events, formulating search strategies, providing translations, and ensuring compliance with data privacy and security. It requires fluency in German and English and proficiency in MS Office. The position is freelance, working at 0.5 Full-Time Equivalent (FTE).

The PV Assistant will be responsible for supporting pharmacovigilance activities and project teams at PrimeVigilance. No previous pharmacovigilance experience required as training will be provided. Responsibilities include managing safety reports, submitting periodic reports, and maintaining documents. Qualifications include advanced English skills, administrative experience, IT skills, attention to detail, and ability to work under pressure.

The PV Administrative Assistant will support pharmacovigilance activities, including receiving and tracking safety messages and reports, maintaining archives, and ensuring compliance with regulations. The role requires good organizational skills and the ability to manage multiple tasks in a dynamic environment.